Potential cytotoxic and apoptosis inducing agents: synthesis and evaluation of methoxy-substituted chalcones against human lung and cervical cancers

被引:0
作者
K. R. Ethiraj
Jesil Mathew Aranjani
F. Nawaz Khan
机构
[1] School of Advanced Sciences,Pharmaceutical Chemistry Division
[2] VIT University,Department of Pharmaceutical Biotechnology
[3] Manipal College of Pharmaceutical Sciences,Organic Chemistry Division
[4] Manipal University,undefined
[5] School of Advanced Sciences,undefined
[6] VIT University,undefined
来源
Medicinal Chemistry Research | 2013年 / 22卷
关键词
Methoxy-substituted chalcones; Cytotoxicity; MTT assay; HeLa; Flow cytometry; Apoptosis;
D O I
暂无
中图分类号
学科分类号
摘要
The role of methoxy group substitution in various positions in both the rings of chalcones on cytotoxicity profile was studied using various synthesized chalcones. The fluorine containing acetophenones when reacted with various methoxy-substituted benzaldehydes in the presence of 10 % sodium hydroxide solution gave the functionalized chalcones. All the synthesized chalcones were confirmed by spectral techniques like FTIR, 1H NMR, 13C NMR, and HRMS studies. All the synthesized compounds were screened for their cytotoxicity against various cell lines. The promising compounds were analyzed for cell cycle analysis.
引用
收藏
页码:5408 / 5417
页数:9
相关论文
共 46 条
  • [41] Novel pyrazole-based COX-2 inhibitors as potential anticancer agents: Design, synthesis, cytotoxic effect against resistant cancer cells, cell cycle arrest, apoptosis induction and dual EGFR/Topo-1 inhibition
    Halim, Peter A.
    Sharkawi, Souty M. Z.
    Labib, Madlen B.
    BIOORGANIC CHEMISTRY, 2023, 131
  • [42] Synthesis of 2,2,4-trimethyl-1,2-dihydroquinolinyl substituted 1,2,3-triazole derivatives: Their evaluation as potential PDE 4B inhibitors possessing cytotoxic properties against cancer cells
    Praveena, K. S. S.
    Durgadas, Shylaprasad
    Babu, N. Suresh
    Akkenapally, Surekha
    Kumar, C. Ganesh
    Deora, Girdhar Singh
    Murthy, N. Y. S.
    Mukkanti, Khagga
    Pal, Sarbani
    BIOORGANIC CHEMISTRY, 2014, 53 : 8 - 14
  • [43] Combretastatin A-4 derivatives: synthesis and evaluation of 2,4,5-triaryl-1H-imidazoles as potential agents against H1299 (non-small cell lung cancer cell)
    Chih-Hua Tseng
    Chi-Yi Li
    Chien-Chih Chiu
    Huei-Ting Hu
    Chein-Hwa Han
    Yeh-Long Chen
    Cherng-Chyi Tzeng
    Molecular Diversity, 2012, 16 : 697 - 709
  • [44] Synthesis and biological evaluation of a series of 2-(3,4,5-trimethoxybenzoyl)-indol-3-yl acetic acid derivatives as potential agents against human leukemia K562 cells
    Romagnoli, Romeo
    Baraldi, Pier Giovanni
    Cruz-Lopez, Olga
    Carrion, Maria Dora
    Cara, Carlota Lopez
    Balzarini, Jan
    Fabbri, Enrica
    Gambari, Robero
    LETTERS IN DRUG DESIGN & DISCOVERY, 2008, 5 (03) : 214 - 220
  • [45] The non-steroidal anti-inflammatory drugs based on Zinc(II) picoline complexes: Synthesis, characterization, and evaluation of antiproliferative effects against human breast adenocarcinoma MDA-MB-453 cells by inducing ROS-mediated apoptosis and down-regulating PI3K/AKT signaling pathway
    Caglar, Sema
    Polat, Tugba
    Altay, Ahmet
    Yeniceri, Esma
    Caglar, Buelent
    POLYHEDRON, 2024, 254
  • [46] Design, synthesis, DFT, molecular modelling studies and biological evaluation of novel 3-substituted (E)-5-(arylidene)-1-methyl-2-thioxoimidazolidin-4-ones with potent cytotoxic activities against breast MCF-7, liver HepG2, and lung A549
    Khodair, Ahmed, I
    Bakare, Safyah B.
    Awad, Mohamed K.
    Nafie, Mohamed S.
    JOURNAL OF MOLECULAR STRUCTURE, 2021, 1229